Alex S Nord
Alex S Nord
Associate Professor, Department of Neurobiology, Physiology, and Behavior and Psychiatry and
Vahvistettu sähköpostiosoite verkkotunnuksessa - Kotisivu
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
T Walsh, JM McClellan, SE McCarthy, AM Addington, SB Pierce, ...
science 320 (5875), 539-543, 2008
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
T Walsh, S Casadei, MK Lee, CC Pennil, AS Nord, AM Thornton, W Roeb, ...
Proceedings of the National Academy of Sciences 108 (44), 18032-18037, 2011
Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas
KP Pennington, T Walsh, MI Harrell, MK Lee, CC Pennil, MH Rendi, ...
Clinical Cancer Research 20 (3), 764-775, 2014
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing
T Walsh, MK Lee, S Casadei, AM Thornton, SM Stray, C Pennil, AS Nord, ...
Proceedings of the National Academy of Sciences 107 (28), 12629-12633, 2010
Rapid and pervasive changes in genome-wide enhancer usage during mammalian development
AS Nord, MJ Blow, C Attanasio, JA Akiyama, A Holt, R Hosseini, ...
Cell 155 (7), 1521-1531, 2013
Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery
JW Gaynor, G Wernovsky, GP Jarvik, J Bernbaum, M Gerdes, E Zackai, ...
The Journal of thoracic and cardiovascular surgery 133 (5), 1344-1353. e3, 2007
Fine tuning of craniofacial morphology by distant-acting enhancers
C Attanasio, AS Nord, Y Zhu, MJ Blow, Z Li, DK Liberton, H Morrison, ...
Science 342 (6157), 1241006, 2013
A high-resolution enhancer atlas of the developing telencephalon
A Visel, L Taher, H Girgis, D May, O Golonzhka, RV Hoch, GL McKinsey, ...
Cell 152 (4), 895-908, 2013
A public gene trap resource for mouse functional genomics
Nature genetics 36 (6), 543-544, 2004
Germline Chd8 haploinsufficiency alters brain development in mouse
AL Gompers, L Su-Feher, J Ellegood, NA Copping, MA Riyadh, ...
Nature neuroscience 20 (8), 1062-1073, 2017
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing
CC Pritchard, C Smith, SJ Salipante, MK Lee, AM Thornton, AS Nord, ...
The Journal of Molecular Diagnostics 14 (4), 357-366, 2012
Accurate and exact CNV identification from targeted high-throughput sequence data
AS Nord, M Lee, MC King, T Walsh
BMC genomics 12, 1-10, 2011
Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndrome
S Tabbutt, AS Nord, GP Jarvik, J Bernbaum, G Wernovsky, M Gerdes, ...
Pediatrics 121 (3), 476-483, 2008
Genomic perspectives of transcriptional regulation in forebrain development
AS Nord, K Pattabiraman, A Visel, JLR Rubenstein
Neuron 85 (1), 27-47, 2015
Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery
S Fuller, AS Nord, M Gerdes, G Wernovsky, GP Jarvik, J Bernbaum, ...
European journal of cardio-thoracic surgery 36 (1), 40-48, 2009
Perioperative stroke in infants undergoing open heart operations for congenital heart disease
J Chen, RA Zimmerman, GP Jarvik, AS Nord, RR Clancy, G Wernovsky, ...
The Annals of thoracic surgery 88 (3), 823-829, 2009
The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse
AS Nord, PJ Chang, BR Conklin, AV Cox, CA Harper, GG Hicks, ...
Nucleic acids research 34 (suppl_1), D642-D648, 2006
Tissue-specific RNA expression marks distant-acting developmental enhancers
H Wu, AS Nord, JA Akiyama, M Shoukry, V Afzal, EM Rubin, ...
PLoS genetics 10 (9), e1004610, 2014
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
D Yan, D Tekin, G Bademci, J Foster, FB Cengiz, A Kannan-Sundhari, ...
Human genetics 135, 953-961, 2016
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
AS Nord, W Roeb, DE Dickel, T Walsh, M Kusenda, KL O'connor, ...
European Journal of Human Genetics 19 (6), 727-731, 2011
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Artikkelit 1–20